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金纳米颗粒上混合肽自组装单分子层中的超分子域

Supramolecular domains in mixed peptide self-assembled monolayers on gold nanoparticles.

作者信息

Duchesne Laurence, Wells Geoff, Fernig David G, Harris Sarah A, Lévy Raphaël

机构信息

School of Biological Sciences and Liverpool Institute of Nanoscale Science, Engineering and Technology, University of Liverpool, Biosciences Building, Crown Street, Liverpool L697ZB, UK.

出版信息

Chembiochem. 2008 Sep 1;9(13):2127-34. doi: 10.1002/cbic.200800326.

Abstract

Self-organization in mixed self-assembled monolayers of small molecules provides a route towards nanoparticles with complex molecular structures. Inspired by structural biology, a strategy based on chemical cross-linking is introduced to probe proximity between functional peptides embedded in a mixed self-assembled monolayer at the surface of a nanoparticle. The physical basis of the proximity measurement is a transition from intramolecular to intermolecular cross-linking as the functional peptides get closer. Experimental investigations of a binary peptide self-assembled monolayer show that this transition happens at an extremely low molar ratio of the functional versus matrix peptide. Molecular dynamics simulations of the peptide self-assembled monolayer are used to calculate the volume explored by the reactive groups. Comparison of the experimental results with a probabilistic model demonstrates that the peptides are not randomly distributed at the surface of the nanoparticle, but rather self-organize into supramolecular domains.

摘要

小分子混合自组装单分子层中的自组织为制备具有复杂分子结构的纳米粒子提供了一条途径。受结构生物学启发,引入了一种基于化学交联的策略,以探测嵌入纳米粒子表面混合自组装单分子层中的功能肽之间的距离。距离测量的物理基础是随着功能肽靠得更近,从分子内交联到分子间交联的转变。对二元肽自组装单分子层的实验研究表明,这种转变发生在功能肽与基质肽的极低摩尔比下。肽自组装单分子层的分子动力学模拟用于计算反应基团所占据的体积。将实验结果与概率模型进行比较表明,肽并非随机分布在纳米粒子表面,而是自组织形成超分子域。

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